CA2703111C - Stable amorphous calcium carbonate comprising phosphorylated amino acids, synthetic phosphorylated peptides, and gastrolith proteins - Google Patents

Abstract

Provided are compositions containing amorphous calcium carbonate (ACC), and at least one phosphorylated amino acid or phosphorylated peptide which stabilizes the amorphous form of said calcium carbonate. Particularly, the peptide can be selected from crustacean proteins, also provided by the invention, namely GAP65, GAP22, GAP21, and GAP12. The compositions are useful in pharmaceutical and nutraceutical formulations.

Description

STABLE AMORPHOUS CALCIUM CARBONATE
COMPRISING PHOSPHORYLATED AMINO ACIDS, SYNTHETIC PHOSPHORYLATED PEPTIDES, AND
GASTROLITH PROTEINS

Field of the Invention The present invention relates to compositions comprising amorphous calcium carbonate, and to methods of preparing same, and further to compositions comprising phosphorylated amino acids or peptides. Particularly, said Io peptides are selected from crustacean proteins, including GAP65, GAP22, GAP21, and GAP 12. Pharmaceutical and nutraceutical compositions comprising amorphous calcium carbonate and phosphorylated amino acids or peptides are provided.

Background of the Invention Calcium plays one of the central roles in the signal transduction, and further it is an important structural element in biological systems. From protozoa to vertebrata, deposited calcium salts helps to keep rigid bodily shapes of animals, calcium phosphate being the main component of endoskeletons in the vertebrates and calcium carbonate of exoskeletons in the invertebrates.
Calcified exoskeletons with calcium carbonate minerals as the main constituents are widespread among echinoderms, mollusks, and arthropods, providing protection and serving as calcium storage. Some crustaceans store calcium carbonate temporarily, in an amorphous state, which makes it better available, particularly for quick mobilization during the mineralization of their new exoskeleton structures after molting. The formation of amorphous calcium carbonate in the living bodies of, for example, crayfish is rather intriguing, since amorphous minerals are usually thermodynamically unstable. Amorphous calcium carbonate (ACC) tends to transform to its crystalline polymorphs, mainly calcite and aragonite. WO 2005/115414

-2-employs crustacean organs for providing compositions with stable ACC which is readily available for human consumption. In view of the general metabolic and biomechanical importance of calcium, and since ACC is a potentially more soluble and absorbable form of calcium carbonate as a dietary supplements, it is an object of the invention to provide new methods for preparing amorphous calcium carbonate.

It is another object of this invention to provide pharmaceutical and nutraceutical compositions comprising stable ACC.

Other objects and advantages of present invention will appear as description proceeds.

Summary of the Invention The present invention relates to a composition comprising amorphous calcium carbonate (ACC) and at least one component selected from phosphorylated amino acids and phosphorylated peptides. Said phosphorylated amino acids and phosphorylated peptides may comprise phospho-serine or phospho-threonine or both. Said phosphorylated amino acids and phosphorylated peptides stabilize the amorphous form of said calcium carbonate in the composition of the invention. In one aspect of the invention, said phosphorylated peptide originates from crustacean gastrolith.
In one embodiment, the composition of the invention comprises ACC, at least one phosphorylated amino acid or peptide, and chitin or chitosan.

In another aspect, the present invention relates to new crustacean peptides and their use in affecting the crystalline state of calcium carbonate and in the preparation of formulations. The invention also relates to functional fragments of said peptides. The isolated proteins related to below include 3o GAP65, GAP22, GAP21, and GAP12 (were GAP stands for gastrolith protein); deduced amino acid sequences of said new proteins are provided

-3-herein, and they are denoted as SEQ. ID. NOS: 1 - 4. The invention provides an isolated and purified crustacean peptide having essentially a sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:9, SEQ ID
NO:17, SEQ ID NO:24, and homologues thereof. A sequence homolog according to the invention is a peptide with any insertions, deletions, and substitutions, as far as at least 90 % of the sequence is preserved. The invention further includes an isolated and purified peptide comprising in its sequence a subsequence, said subsequence being a fragment of the above said crustacean GAP peptides, preferably a subsequence at least ten amino acid long. Said subsequence may have a sequence selected from, for example, SEQ
ID NOS: 2 to 8, SEQ ID NOS: 10 to 16, and SEQ ID NOS: 18 to 23, or other fragments of sequences SEQ ID NO:1, SEQ ID NO:9, SEQ ID NO:17, SEQ ID
NO:24. The invention provides a composition comprising one or more peptides as defined above, or their derivatives or variants or functional fragments or mixtures thereof, together with amorphous calcium carbonate (ACC). Said peptide stabilizes the amorphous form of said calcium carbonate in said composition. The term "functionally equivalent fragment, derivative, or variant" as used herein includes peptides with modifications that do not interfere with their ability to inhibit calcium carbonate crystallization.

The invention is directed to a peptide having amino acid sequence selected from SEQ ID NO:1, SEQ ID NO:9, SEQ ID NO:17, and SEQ ID NO:24, and to peptides being their sequence homologous having, preferably, at least 90%
homology. A DNA sequence encoding a peptide according to the invention is a part of the invention as well. Provided in the invention is a calcium carbonate preparation containing a peptide as defined above or its derivative.
In a preferred embodiment of the invention, a calcium carbonate preparation comprising ACC is provided, said preparation being stable at least for one month. A method of preparing stable amorphous calcium carbonate is disclosed, which comprises mixing in aqueous phase in any order a soluble salt comprising calcium, a carbonate source, and a phosphorylated amino

-4-acid or phosphorylated peptide. Said source may, for example, comprise a carbonate salt dissolved in the liquid phase, or said source may comprise gaseous carbon dioxide.

The invention provides a pharmaceutical formulation comprising the above said composition, containing one or more phosphorylated amino acids, or phosphorylated peptides as defined herein or their derivatives or variants or functional fragments or mixtures thereof, together with ACC. The above said composition is, in other aspect of the invention, advantageously used as a 1o nutraceutical formulation, for example as a food additive. Said pharmaceutical formulation is preferably orally administered and may comprise fillers or solvents or additives. Said pharmaceutical formulation is preferably used in treating conditions selected from the group consisting of pain, proliferative diseases, neurological disorders, immunologic disorders, cardiovascular diseases, pulmonary diseases, nutritional disorders, reproductive disorders, musculoskeletal disorders, and dental problems. Said treating may lead to disappearance of causative factors or to mitigating the symptoms. Said proliferative disease may be, for example, breast carcinoma or bronchogenic carcinoma. Said treating may comprise slowing down or inhibiting the cell proliferation in a tumor. As for said pain, it may be postoperative pain, pain after injury, pain associated with, cancer, and neuropathic pain. The mentioned neurological disorder is, for example, selected from demyelinating diseases, dementias, and movement disorders.
Said condition may be a degenerative disease selected from multiple sclerosis, Alzheimer's disease, and Parkinson's disease. Said condition may comprise a bone or bone marrow disorder, which may be, for example fracture or osteoporosis. Said condition may be a neurodegenerative disorder.
Said new peptides GAP65, GAP22, GAP21, and GAP12 or their derivatives 3o are used, in one aspect of the invention, in the manufacture of medicaments.
Also provided is a method of treating a bone disorder or injury, and a method of managing pain, comprising orally administering a formulation comprising

-5-calcium carbonate and one or more of said new peptides or their derivatives.
The term "derivatives" as used herein includes also peptide products obtained by alkylation, esterification, neutralization, cyclization, or oligomerization.
The invention provides a method of inhibiting the crystallization of calcium carbonate in a mixture comprising a carbonate and a calcium salt, comprising admixing into said mixture an amount of a phosphorylated amino acid or a phosphorylated peptide. Said phosphorylated amino acid or a Io phosphorylated peptide preferably comprises phospho-serine or phospho-threonine. The invention provides, in one embodiment, a method of inhibiting the crystallization of calcium carbonate, comprising admixing into the crystallization or precipitation mixture an amount of a peptide having a sequence selected from SEQ ID NO:1, SEQ ID NO:9, SEQ ID NO:17, and SEQ ID NO:24, or its homolog or functional fragment or derivative or variant, or of a mixture thereof. A method of inhibiting the crystallization of calcium carbonate according to the invention is provided, comprising providing a calcium salt soluble in water, and contacting said salt with a peptide selected from GAP65, GAP22, GAP21, and GAP12, or with its functionally equivalent fragment, derivative, or variant thereof, or with a mixture thereof.

In one aspect of the invention, food additives or functional foods are provided, comprising a mixture of calcium carbonate and a phosphorylated amino acid or peptide; said peptide, in one embodiment, having a sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:9, SEQ ID NO:17, SEQ ID
NO:24, and homologues or fragments thereof.

Brief Description of the Drawings 3o The above and other characteristics and advantages of the invention will be more readily apparent through the following examples, and with reference to

-6-the appended drawings, wherein:
Fig. 1. shows the isolation of gastrolith soluble proteins, purification and partial sequencing of GAP65; Fig. 1A - SDS-PAGE Coomassie staining of the soluble proteins profile of the gastrolith, compared to molecular weight reference proteins (left), SDS-PAGE of fraction 17 containing GAP65 purified by DEAE column chromatography stained with Coomassie, "stains all", and "pas" (right); Fig. 1B -chromatogram of GAP65 obtained by nanospray Qtof2 following tryspin digestion, sequences of the peptides from significant peaks were obtained through MSIMS analysis;
Fig. 2. comprises the complete deduced amino acid sequence of GAP65 and it bioinformatic analysis; Fig. 2A - deduced amino acid sequence of the open reading frame of GAP65, in bold is predicted signal sequence, grey boxes are possible phosphorylation sites, dark boxes at amino acids no. 72 and 173 are predicted 0-glycosylation sites, light boxes are predicted N-glycosylation sites; Fig. 2B - a scheme of the GAP65 sequence showing the predicted domains: ChtBD2 is chitin binding domain 2, LDLa is low-density lipoprotein receptor domain class A, and the last one is polysaccharide deacetylase domain; Fig. 2C - 3D structure of the LDLa domain based on homology to lipoprotein receptor, on the left is the NMR structure of complement-like repeat CR3 from the low density lipoprotein receptor-related protein, on the right is the predicted structure of the LDLa domain of GAP65;
Fig. 3. shows specific expression of GAP65 and its localization in the columnar epithelium of the gastrolith during induced premolt; Fig.
3A - detection of GAP65 expression during premolt using RT-PCR, RNA was sampled from gastrolith epithelial disc, hepatopancreas, sub-epidermal tissue, sperm duct, and stomach wall, elongation factor 2 (Eft2) was used to reassure RNA extraction, control for genomic contamination was used; Fig. 3B - localization of GAP65 expression by in situ hybridization in induced premolt and intact

7 PCT/IL2008/001362 intermolt males, left panel represents the hematoxylin and eosin staining (H&E), middle panel represents the negative control sense -GAP65 probe, the two right panels represent the GAP65 anti-sense probe with the last being an enlargement of a specific area, the bar represents 200 m except for induced premolt sense probe where the bar represents 100 gm;
Fig. 4. shows relative transcript level of GAP65 (denoted GASP 65) in the gastrolith disc following GAP65 silencing, relative quantitation of GAP65 transcript level using real-time RT-PCR in the gastrolith disc of crayfish injected with (left to right): ecdysone and dsRNA of GAP65, ecdysone and dsRNA carrier, ecdysone and dsRNA of C. quadricarinatus vitellogenin (CqVg), ecdysone carrier and dsRNA
carrier, and the letters represent statistical significance;
Fig. 5. are photos showing morphological deformities of the gastroliths following GAP65 silencing, representative gastroliths are dissected from crayfish injected with either of ecdysone and dsRNA of GAP65 (left), ecdysone and dsRNA carrier (middle), ecdysone carrier and dsRNA carrier (right); Fig. 5A - lateral view of whole gastroliths dissected from the crayfish; Fig. 5B and 5C - X-ray imaging of the above gastrolith prior to dissection (dorsal view);
Fig. 6. shows scanning electron microscope (SEM) micrographs of gastroliths structural deformities following GAP65 gene silencing;
representative gastroliths were dissected from crayfish injected with ecdysone + GAP65 dsRNA (left) and ecdysone + dsRNA carrier (right); Fig. 6A and 6B - cross sections of the central part of the gastrolith demonstrating the mineral and matrix arrangement (X
50, X 200, respectively); Fig. 6C - mineral arrangement comprising nano-spherules (X 15000); the ecdysone without GAP shows normal gastrolith appearance, while the ecdysone + GAP65 dsRNA treated gastrolith appears deformed;

-8-Fig. 7. shows SEM images of in vitro precipitated calcium carbonate in the presence/absence of the gastrolith purified protein; Fig. 7A -calcium carbonate precipitate with GAP65 enriched fraction (left), calcium carbonate precipitated with equivalent amount of trypsin as a control (right); Fig. 7B - a SEM image of ACC 40 days after the precipitation, demonstrating typical amorphous structures with nanospheres of 50-500 nm;
Fig. 8. shows Raman spectra of the ACC obtained by precipitation with GAP65 enriched fraction; Fig. 8A - Raman spectra of calcium carbonate obtained by precipitation with GAP65 enriched fraction;
Fig. 8B - 27 days after the precipitation; Fig. 8C - 6.5 month after the precipitation;
Fig. 9. is a comparison of the Raman spectra (around the 1085 peak) of 6.5-month old ACC (induced by GAP65) with calcite;
Fig. 10. shows partial sequencing of gastrolith proteins, presented are chromatograms obtained by nanospray Qtof2 following tryspin digestion, sequences of the peptides from significant peaks were obtained through MS/MS analysis; Fig. 10A shows GAP22; Fig. 10B
shows GAP21; Fig. 10C shows GAP12;
Fig. 11. shows Raman spectra of the calcium carbonate precipitated from the solution of calcium chloride and sodium carbonate in the presence of gastrolith extract;
Fig. 12. is Table 1, showing amino acid compositions of GAP proteins;
Fig. 13. shows nucleotide sequence of GAP22 cDNA and the corresponding deduced amino acid sequence in open reading frame; the asterisks indicate stop codons and the gray highlighted sequences are the untranslated regions; the putative signal peptides in the N-terminus are underlined;
Fig. 14. shows nucleotide sequence of GAP21 cDNA and the corresponding deduced amino acid sequence in open reading frame; the symbols have the same meaning as in Fig. 13; and

-9-Fig. 15. relates to the GAP sequences; Fig. 15A shows nucleotide sequence of GAP12 cDNA and the corresponding deduced amino acid sequence in open reading frame; the symbols have the same meaning as in Fig. 13; Fig. 15B is sequence alignment of GAP 12 and GAP21, amino acid positions of the two proteins are shown on the right and left, sequence identities are indicated by "*", conserved substitutions are indicated by ":", and semi-conserved substitutions are indicated by Fig. 16. to Fig. 27 show Raman Spectra described in detail in Examples 9 to 20; and Fig. 28 to Fig. 32 show Raman Spectra of samples prepared according to Examples 9, 10 and 18-20, respectively, which were stored after the precipitation at room temperature as described.

Detailed Description of the Invention It has now been found that some phosphorylated amino acids or peptides affect the precipitation of calcium carbonate in vitro, leading to the formation of amorphous form of calcium carbonate. Particularly, the effects have been observed when said peptides comprise several proteins present in the late premolt gastrolith of Cherax quadricarinatus. Peptides having apparent molecular weights of approximately 65 kDa, 22 kDa, 21 kDa, and 12 kDa induce precipitation of nanospheres of amorphous calcium carbonate material; in comparison, an inert protein provides CaCO3 crystals. The nanoparticles show a Raman shift typical for amorphous CaCO3.

The above proteins, denoted as GAP65, GAP22, GAP21, GAP 12, respectively, according to their apparent molecular weights estimated by SDS-PAGE, are involved in the precipitation and stabilization of ACC. The gastrolith extract which contains said four proteins inhibits calcium carbonate crystallization 3o and stabilizes the amorphous form of calcium carbonate (ACC). ACC was detected by Raman spectrometry in a precipitate of CaCO3 prepared from a

-10-solution containing CaC12, Na2CO3 and the gastrolith extract (Fig. 11). The presence of ACC is validated by the presence of a predominant peak at about 1080cm-1. Expressions of the GAP genes were found to be specific to the gastrolith epithelial disc and sub-epidermal tissue, both are cuticle related tissues. Specific expressions of the GAP peptides in several target tissues by means of RT-PCR was also studied. For example, the expression of GAP65 was found in more cuticle related tissues, whereas the expression of GAP22 was found rather in the gastrolith epithelial disc.

io The cDNA sequences of the corresponding genes were obtained and their deduced proteins were found (Figs. 2, 13-15). All four proteins were found to contain signal peptides at their N-terminus (underlined amino acids in Figs.
13-15, bold in Fig. 2). Similarity search against databases of conserved domains revealed that GAP65 contains three conserved domains: Chitin-binding domain 2, Low density lipoprotein receptor domain class A, and Polysaccharide deacetylase domain. GAP 12, GAP 21 and GAP 22, on the other hand, show no significant similarity to any known domain. Blast alignment of GAP 12 and GAP 21 revealed a 46.3% identity in the deduced amino acid sequences of these proteins (Fig. 15). Physico-chemical analysis of the deduced proteins revealed, that the calculated molecular weights of GAPs 12, 21 and 65 are smaller than expected, 9.9, 19.5 and 60.8 kDa respectively, while that of GAP 22 is higher than expected, 28.6 kDa (Table 1). GAP 12, GAP 21 and GAP 65 have an acidic pI, therefore they are negatively charged at the physiological pH of the gastrolith (near pH 8.5). GAP 12 and GAP 21 have a high percentage of non-polar, aliphatic amino acids (glycine, alanine and valine) and a high percentage of the polar but uncharged amino acid proline (highlighted in gray in Table 1). GAP65 has a high content of acidic amino acids. GAP22 has a basic pI, therefore it is positively charged at the physiological pH of the gastrolith. Its main characteristics are a. high percentage of the polar but uncharged amino acid proline and of the positively charged arginine.

-11-Due to special features of the new proteins, provided in this invention is also a method of inhibiting the crystallization of calcium carbonate, comprising admixing into the crystallization or precipitation mixture an amount of GAP65 or a functional fragment thereof, or a derivative, or a variant thereof.
In other aspect of the invention, a method is provided of inhibiting the crystallization of calcium carbonate, comprising contacting a calcium salt soluble in water with GAP65 or a functional fragment, derivative, or variant thereof.

io GAP65 was purified from gastrolith soluble protein extract by ion exchange chromatography, and was identified as a negatively charged glycopeptide, containing about 12 mol% Asp + Glu, based on SEQ. ID. NO. 1. Sequencing of the peptides by MS-MS provided seven oligopeptide subsequences (SEQ.
ID. NO. 2-8; Fig. 1B) which were used for the construction of degenerative primers for the acquisition of a complete GAP65 encoded gene sequence based on gastrolith epithelial disc mRNA. The total deduced amino acid sequence revealed a 548 amino acids long peptide (SEQ. ID. NO. 1; Fig. 2A).
Bioinformatic analysis of GAP65 sequence suggested the presence of three known domains (Fig. 2B): chitin binding domain 2 (ChtBD2) from amino acids 29-102, low-density lipoprotein receptor domain class A (LDLa), from amino acids 122-159, and polysaccharide deacetylase domain from amino acids 195-332. The LDLa domain has a predicted calcium binding property.
Expression of GAP65 was tested in premolt crayfish in several target tissues by means of RT-PCR, and was detected in the gastrolith epithelial disc and in the sub-epidermal tissue, both are cuticle related tissues (Fig. 3A). In situ hybridization visualized the localization of the GAP65 expression in the gastrolith disc of induced premolt and intact intermolt crayfish (Fig 5B).
Relative GAP65 transcript levels in the gastrolith epithelial disc following silencing using GAP65 dsRNA were measured using realtime RT-PCR (Fig.
4). The role of GAP65 in gastrolith formation was tested by an RNAi technique using in vivo injections of GAP65 dsRNA to intermolt crayfish

-12-(Fig. 5). The initiation of gastrolith formation was achieved by injection of ecdysone. Morphological deformities of the gastrolith can be observed in crayfish injected with both GAP65 dsRNA and ecdysone (Fig. 5A shows dissected gastrolith, Fig. 5B and 5C are X-ray views).

It was found that GAP65 essentially affects the micro structure of the crayfish gastrolith. Scanning electron microscope (SEM) micrographs of gastroliths dissected from crayfish injected either with GAP65 dsRNA
together with ecdysone or only with ecdysone revealed severe structural 1o abnormalities caused by the absence of GAP65 (Fig.6). The packaging of the ACC in spherules, and the spherules size, is important for the dense packaging of the gastrolith; the absence of GAP65 led to larger spherules and less condensed structure when compared to the normal gastrolith.

In order to elucidate the role of GAP65 in the biomineralization process, an in vitro calcium carbonate precipitation was performed to test the stabilization of ACC. Electron microscope images of the precipitates distinctly indicated different polymorph composition of calcium carbonate for the precipitation in the presence/absence of GAP65-enriched fractions (Fig. 7). The precipitation of calcium carbonate in the absence of GAP, namely in the presence of an inert protein, resulted in rapid crystallization providing crystals of calcite and/or vaterite as large as 10 m. On the other hand, the precipitation of calcium carbonate in the presence of GAP65 resulted in amorphous CaCO3 observed as a thin layer consisting of 40-60 nm spherules. The amorphous nature of the calcium carbonate in said spherules was corroborated by Raman spectra, which showed the distinct ACC peak at 1070 cm-1, and further by employing powder x-ray diffraction (XRD), which indicated the absence of diffracting peaks from crystalline materials. The presence of GAP65 in the ACC spherules formed by the in vitro precipitation was confirmed by purification of the protein from the spherules and its identification by SDS-PAGE.

-13-CaCO3 deposits obtained by precipitation in the presence of GAP65 were initially characterized by polarized microscope, identifying calcite, vaterite, and ACC. The observations were confirmed by Raman spectroscopy and powder XRD. The ACC constituted about at least 50% of the total CaCO3.
The ACC remained stable under room condition for at least 1 months.

The invention, thus, provides new proteins associated with calcium metabolism in crayfish, which affect the crystalline state of calcium carbonate. Provided is a method of inhibiting the crystallization of calcium carbonate, comprising admixing into the crystallization or precipitation mixture an amount of GAP proteins or functionally equivalent fragments thereof, or derivatives, or variants thereof. The invention relates to a method of preparing ACC by admixing said new protein into a precipitation mixture, namely into a mixture in which the precipitation of CaCO3 occurs, and in which precipitation of crystalline material would occur without said protein.
A nonlimiting example of such mixture includes an aqueous solution of calcium chloride comprising GAP65 into which a sodium carbonate solution is added. Of course the order of mixing the components may change, as well as the types of the ions sources. The concentration of GAP65 in the mixture may be, for example, about from 0.05 to 5 wt% based on the weight of CaCO3.
The concentration of GAP65 in the precipitation mixture may be, for example, about from 1 to 100 g/ml.

The instant invention provides a composition containing ACC and a phosphorylated amino acid or peptide, for example a GAP protein. In an important aspect of the invention, a formulation is provided for treating disorders associated with calcium metabolism or signaling, comprising ACC
and a stabilizing amount of phosphorylated amino acid or peptide, for example a GAP protein or its derivatives. The formulation is preferably used for oral administration. The formulation of the invention is used as a

-14-therapeutic means, or as a therapeutic supplement, or as a nutritional supplement.

In a preferred embodiment of the invention, ACC prepared according to the invention is comprised in a formulation for treating conditions associated with calcium metabolism or calcium signaling. Said conditions may be selected from the group consisting of pain, proliferative diseases, neurological disorders, immunologic disorders, cardiovascular diseases, pulmonary diseases, nutritional disorders, reproductive disorders, musculoskeletal 1o disorders, and dental problems. Said treating may comprise mitigating the symptoms of the diseases. Said proliferative disease may be selected from sarcomas, carcinomas, lymphomas and melanomas. Said carcinoma is, for example, breast carcinoma or bronchogenic carcinoma. Said treating may lead to shrinking tumors, stopping their growth, or slowing down or inhibiting the cell proliferation in the tumors. Said pain may be selected from postoperative pain, pain after injury, pain associated with cancer, and neuropathic pain. Said neurological disorder may be selected from demyelinating diseases, dementias, and movement disorders; said disorders being, for example, multiple sclerosis, Alzheimer's disease, Parkinson's disease, or other degenerative disease. Said condition to be treated may comprise a bone or bone marrow disorder, such as fracture or osteoporosis. In a preferred embodiment, a composition of the invention is used for treating a neurodegenerative disorder.

The invention relates to a composition of matter comprising ACC and a stabilizing amount of a phosphorylated amino acid (PAA) or a phosphorylated peptide (PP), for example a composition comprising one or more PAA, or one or more PP such as GAP peptides or their functional fragments, derivatives, or variants. The invention also relates to ACC
stabilized with PAA, or PP such as GAPs, for use as a medicament or in the manufacture of a medicament, or for use as a food additive.

-15-The process for the preparation of ACC may comprise the steps:
i) Forming an aqueous solution with calcium ions (with CaC12 solution).
ii) Addition of soluble or insoluble "additives" (phosphoamino acids, chitosan, chitin, synthetic peptides, phosphorylated peptides/proteins or fragments thereof, etc.).
iii) Addition of carbonate ions (with Na2CO3 solution or another carbonate source, like for example C02, or (NH4)2CO3).
iv) Agitation.
v) Precipitation of CaCO3 slurry (by centrifugation, filtration etc.).
1o vi) Slurry dehydration (by lyophilizer, air flow, spray drying etc.).
Analysis of the product may comprise testing the resultant CaCO3 by various methods (as XRD, electron diffraction, SEM) to verify its amorphous nature.
Raman spectroscopy (RS) was found to be the most efficient and reliable method to characterize ACC. The Raman shifts characteristics of the mineral reported here are the carbonate peak at 1080 cm-1 whose broad shape is indicative of ACC and proportional to its content. The phosphate peak at 950 cm-1, is proportional to the phosphate content in the sample. Yet, the ratio between 1080 to 950 cm-1 is proportional, but not directly indicative of the C032-/PO43- ratio.

Calcium and carbonate ions, in the solutions from which calcium carbonate was precipitated, was usually in the range of from about 10mM to about 500mM. The molar ratio of phosphorylated amino acid (PAA) to calcium was usually in the range of 0.01-0.5. A higher concentration of PAA inhibited the spontaneous precipitation. The chitosan, when present, was in the range of 0.03-0.3 wt%.

Peptides which were extracted from demineralized Cherax gastroliths by different proteolytic enzymes (trypsin, papain, and Streptomyces protease) induced the formation of ACC. It is suggested that phosphoamino acids and phosphopeptides can induce ACC formation and can stabilize it. It is possible

-16-that the intact proteins have additional functions. The Raman spectra and EDS analysis show a significant amount of calcium phosphate similar to the ACC induced by total insoluble matrix (ISM), suggesting that the phosphate in the ISM is associated to the proteins.

The precipitated calcium carbonate was checked over long periods for the amorphous/crystalline state. It was found that the samples of ACC obtained by methods of the invention were stable at room temperature for more than seven months, keeping their amorphous state.

Examples Example 1 Gastroliths of Cherax quadricarinatus were prepared as described [WO
2005/1154141. SDS-PAGE separation of soluble proteins from late premolt gastroliths revealed the presence of at least 6 prominent distinct proteins (Fig. 1A left) with the most abundant being at the size of approximately 65 kDa (gastrolith protein 65, GAP65). Further purification of GAP65 from the entire gastrolith soluble proteins content was performed using DEAE
chromatography HPLC with NaCl gradient of up to 1M. GAP65 elution began at 300 mM NaCl but continued mainly at 600 mM (fraction 17). The GAP65 enriched fraction 17 was analyzed by SDS-PAGE and stained with Coomassie (non specific protein staining), "stains all" (negatively charged protein staining), and "pas" (glycoprotein staining), as shown in Fig 1A
right.
These staining suggest that GAP65 is the primary protein in this enriched fraction and it is a negatively charged glycoprotein. Trypsin digestion of GAP65 followed by separation using nanospray Qtof2 and sequencing of the peptides using MS-MS generated 7 predicted peptide sequences (Fig. 1B) which were used for the construction of degenerative primers for the acquisition of a complete GAP65 encoded gene sequence based on gastrolith 3o epithelial disc mRNA. Fig. 2A demonstrates the deduced amino acid sequence of GAP65 open reading frame showing a predicted signal sequence

-17-of the N-terminus of the protein (bold). Approximately 4.6% of total amino acids of GAP65 were predicted as possible phosphorylation sites (grey boxes), whereas only three predicted N-glycosylation sites (light boxes including three letters), and two predicted O-glycosylation sites (dark boxes at amino acids no. 72 and 173) were found. The negative charge originates in part from the acidic residues aspartic and glutamic acids, which comprise about 12 mol% of the protein. Bioinformatic analysis of GAP65 sequence suggested the presence of three known domains (Fig. 2B): chitin binding domain 2 (ChtBD2) from amino acids 29-102, low-density lipoprotein receptor domain 1o class A (LDLa) from amino acids 122-159, and polysaccharide deacetylase domain from amino acids 195-332. Fig. 2C reveals the predicted 3D structure of the LDLa domain based on the homology to NMR structure of complement-like repeat CR3 from the low density lipoprotein receptor-related protein.
This LDLa domain is the only known domain in GAP65 which has a predicted calcium binding property.

Example 2 Specific expression of GAP65 was tested in premolt crayfish in several target tissues by means of RT-PCR (Fig. 3A). The expression of GAP65 was detected in the gastrolith epithelial disc and in the sub-epidermal tissue, both are cuticle related tissues. Expression of GAP65 was not detected in the hepatopancreas, stomach wall, and sperm duct. Localization of GAP65 expression in the gastrolith disc of induced premolt and intact intermolt crayfish by in situ hybridization is presented in Fig 3B. Left panel represents hematoxylin and eosin staining of the gastrolith disc, middle panel is the control sense probe where no expression is detected. The two right panels represent the anti-sense probe with the last being an enlargement of a specific area. The anti-sense probe reveals that the expression of GAP65 can be detected only in the columnar epithelial cells of the gastrolith disc of an induced crayfish, whereas, in intact intermolt crayfish this expression was not detected.

-18-Example 3 Relative GAP65 transcript levels in the gastrolith epithelial disc following silencing using GAP65 dsRNA were measured using realtime RT-PCR and presented in Fig. 4. GAP65 levels were evaluated in crayfish injected with ecdysone and GAP65 dsRNA, ecdysone and dsRNA carrier, ecdysone and C.
quadricarinatus vitellogenin (CqVg) dsRNA, and a control injected with both carriers. CqVg, an hepatopancreatic specific gene found mostly in reproductive females, served as a control for sequence specific silencing.
Transcript levels of crayfish injected with ecdysone and GAP65 dsRNA were 1o significantly lower than the levels found in the ecdysone and dsRNA carrier injected. In the crayfish injected with ecdysone and CqVg dsRNA, GAP65 transcript levels were similar to the levels detected in the ecdysone and dsRNA carrier injected group. In the control carriers injected crayfish GAP65 transcript levels were higher than the levels found in the ecdysone and GAP65 dsRNA injected crayfish but lower than the levels detected in both the ecdysone and dsRNA injected, and the ecdysone CqVg dsRNA injected crayfish. However, the control carriers group was not statistically significantly different from the three other groups.

Example 4 In order to test the role of GAP65 in gastrolith formation, an RNAi technique using in vivo injections of GAP65 dsRNA to intermolt crayfish was applied.
The initiation of gastrolith formation was achieved by injection of ecdysone.
In Fig. 5 gastrolith of crayfish injected with either ecdysone + GAP65 dsRNA, ecdysone + dsRNA carrier, or with carriers of both ecdysone and dsRNA can be seen. Fig. 5A is a lateral view of a representative gastrolith dissected from each treatment group. From this image morphological deformities of the gastrolith can be observed in crayfish injected with both GAP65 dsRNA and ecdysone, whereas in crayfish injected with only ecdysone and dsRNA
carrier, the gastrolith appeared normal with no deformities. In the control carriers injected the gastrolith appeared undeveloped or in an initial growth

-19-stage. Fig. 5B depicts dorsal X-ray view of the crayfish and gastrolith prior to dissection whereas Fig. 5C presents more contrast images of the images of panel B. In crayfish injected with both GAP65 dsRNA and ecdysone, some regions in which less dense detection of mineral is recoded while the gastrolith disc shape structure was retained. In the ecdysone + dsRNA
carrier injected crayfish, the gastrolith appeared normal with no effects on mineral densities. The control carrier gastrolith was too small to be detected by the X-ray imaging.

Example 5 Scanning electron microscope (SEM) images of gastroliths dissected from crayfish injected with GAP65 dsRNA and ecdysone, and from crayfish injected only with ecdysone and dsRNA carrier, are presented in Fig. 6. Fig.
6A-B depict images of a cross section through the central part of the gastrolith. In gastrolith of crayfish injected with GAP65 dsRNA and ecdysone severe structural abnormalities can be observed when compared with the gastrolith of ecdysone and dsRNA carrier only injected crayfish. The dense mineral layered structure observed in the gastrolith of ecdysone and carrier injected is replaced with a loosely packed columnar mineralization structure, which resembles hollow straws, in the gastrolith of ecdysone and GAP65 dsRNA injected crayfish. The packaging of the ACC in spherules, and the spherules size, is important for the dense packaging of the gastrolith.
X15000 magnification comparing the spherules size between the two treatments is presented in Fig. 6C. In the less densely arranged gastrolith of crayfish injected with ecdysone and GAP65 dsRNA spherule size ranged between approximately 100-300 nm whereas in the normal ACC deposited in gastrolith of crayfish injected with ecdysone and dsRNA carrier the spherules have narrower size distribution, ranged from 40-60 run.

-20-Example 6 In order to elucidate the role of GAP65 in the biomineralization process, an in vitro calcium carbonate precipitation essay testing the stabilization of ACC was established. Fig. 7 presents precipitation results of calcium carbonate in the presence of GAP65 and in the presence of other protein (trypsin). SEM images in Fig. 7A indicate the distinct polymorph of calcium carbonate in each treatment. Precipitation of calcium carbonate in the presence of GAP65 resulted in the deposition of an amorphous form (ACC), observed as a thin layer comprised of 100-500 nm spherules. Precipitating 1o experiments performed under the same conditions but in the presence of trypsin resulted with rapid crystallization, observed as large 10 m single crystals of calcite and vaterite spherulites. Fig. 7B confirms the nature of the ACC in calcium carbonate precipitated in the presence of GAP65. Raman analysis is showing the distinct spectra of ACC with a clear broad peak at 1070 cm-1. The presence of GAP65 in the ACC spherules formed by the in vitro precipitation was confirmed by purification of the protein from the mineral fraction of the precipitate and its evaluation by SDS-PAGE against the original GAP65 enriched fraction.

Example 7 The stability of ACC precipitated - with - GAP65- was- tested by Raman spectroscopy in the samples held at room temperature. 100 1 of 1M CaC12 was added to 10ml double distilled water (final concentration: 10mM). 80 l from the protein extraction solution (1.2 g/ l) were added (final concentration -10 g/ml). l000 of 1M Na2CO3 (final concentration: 10mM) was added following an intensive shaking. The vial was centrifuged for 5 min at 4000 rpm, the precipitate was smeared over a glass slide and instantly dried with air flow. The CaCO3 deposits were initially characterized by polarized microscope as a mixture of calcite, vaterite, and ACC. The observations were confirmed by Raman spectroscopy. The ACC was in a form of a thin "crust", and it was estimated to comprise about at least 50% of the

-21-total CaCO3. The ACC remained stable at room temperature for at least 1 months, as Raman spectra of the ACC one day after precipitation, 27 days after precipitation, and 6.5 month after precipitation show (Fig. 8A, 8B, 8C).
Comparison of the Raman spectra (around the 1085 peak) of 6.5-month old ACC with calcite (Fig. 9) indicated mixture seemingly comprising ACC and vaterite (when considering a shoulder on the 1085 peak possibly being an onset of peak splitting characterizing vaterite).

Example 8 1o The gastrolith extract inhibits calcium carbonate crystallization and stabilizes the amorphous form of calcium carbonate (ACC). ACC was detected by Raman spectrometry in a precipitate of CaCO3 prepared from a solution containing CaC12, Na2CO3 and the gastrolith extract (Fig. 11). The presence of ACC is validated by the presence of a predominant broad peak at about 1080cm-1. The peak at 560 is attributed to the glass substrate. Expressions of the GAP genes were found to be specific to the gastrolith epithelial disc and sub-epidermal tissue, both are cuticle related tissues. Specific expression of GAP21, GAP22 and GAP65 in several target tissues was checked by means of RT-PCR, similarly as described in Example 2. GAP21 and GAP65 expressions were found in both cuticle related tissues. GAP22 expression was found only in the gastrolith epithelial disc. The cDNA sequences of the corresponding genes were obtained and their deduced proteins were found (Figs. 13-15). All four proteins were found to contain signal peptides at their N-terminus (underlined amino acids in Figs. 13-15 and bold in Fig. 2).
Similarity search against databases of conserved domains revealed that GAP65 contains three conserved domains; Chitin-binding domain 2, Low density lipoprotein receptor domain class A and Polysaccharide deacetylase domain. GAP 12, GAP21 and GAP22, on the other hand, show no significant similarity to any known domain.

Blast alignment of GAP12 and GAP21 revealed a 46.3% identity in the deduced amino acid sequences of these proteins (Fig. 15B).

-22-Physico-chemical analysis of the deduced proteins revealed, that the calculated molecular weights of GAPs 12, 21 and 65 are smaller than expected, 9.9, 19.5 and 60.8 kDa respectively, while that of GAP22 is higher than expected, 28.6 kDa (Table 1, Fig. 12). GAP12, GAP21 and GAP65 have an acidic pI, therefore they are negatively charged at the physiological pH of the gastrolith (near pH 8.5). GAP12 and GAP21 have a high percentage of non-polar, aliphatic amino acids (glycine, alanine and valine) and a high percentage of the polar but uncharged amino acid proline (highlighted in gray in Table 1). GAP65 has a high content of acidic amino acids, but no io other distinguishable characteristic. GAP22 has a basic pI, therefore it is positively charged at the physiological pH of the gastrolith. Its main characteristics are a high percentage of the polar but uncharged amino acid proline and of the positively charged arginine. According to bioinformatic analysis, GAP 12 and 21 show some similarities in amino acid composition to other proteins known to be involved in calcium precipitation in crustaceans.
Example 9 100 l of 1M CaC12 were added to 10ml double-distilled water (DDW), attaining the final concentration of 10 mM. 200 l of P-serine (P-Ser) solution (100 mM) were added to the solution, attaining 2 mM of P-Ser. 100 l of 1M
Na2CO3 (final concentration: 10mM) were added following an intensive shaking. The vial was centrifuged for 5 min at 4000 rpm at room temperature. The upper solution was removed and the precipitation was smeared over a glass slide and instantly dried by air flow. RS showed ACC
(Fig. 16). The sample was stored at room temperature and tested for ACC
stability five months after the precipitation (Fig. 28).

Example 10 100 l of 1M CaC12 were added to 10ml DDW (final concentration: 10mM).
100 l of P-threonine (P-Thr) solution (100mM) were added to the solution, attaining 1 mM P-Thr. 100 l of 1M Na2CO3 (final concentration: 10mM)

-23-were added following an intensive shaking. The vial was centrifuged for 5 min at 4000 rpm at room temperature. The upper solution was removed and the precipitation was smeared over a glass slide and instantly dried by air flow. RS showed ACC (Fig. 17). The sample was stored at room temperature and tested for ACC stability 4.5 months after the precipitation (Fig. 29).
Example 11 100 l of 1M CaC12 were added to 10 ml DDW (final concentration: 10mM).
200 l of P-serine solution (100mM) were added to the solution. 100 l of 1M
1o Na2CO3 (final concentration: 10mM) were added following an intensive shaking. The vial was centrifuged for 5 min at 4000 rpm at room temperature. The upper solution was removed and the precipitation was frozen in liquid nitrogen and freeze dried in a lyophilizer. RS showed ACC
(Fig. 18).

Example 12 The conditions as described in Example 11 were modified by changing the final concentrations of CaC12 and Na2CO3 from 10 mM to 100 mM. RS
showed ACC (Fig. 19).

Example 13 The conditions as described in Example 10 were modified by changing the dehydration method from flowing air to lyophilizing. RS showed ACC (Fig.
20).

Example 14 A system comprising 20 mM CaC12, 20 mM Na2CO3, 2 mM P-Ser with chitosan (3 wt% Dissolved in 0.2 M acetic acid) that was added to the precipitation solution, after the calcium addition to a final concentration of 0.
3 wt%. RS showed ACC (Fig. 21).

-24-Example 15 The conditions as described in Example 14 were modified by employing the final concentrations of 0.5 M CaC12, 0.5 M Na2CO3, and 3 mM P-Ser. This composition represents the upper concentration limit. RS showed ACC (Fig.
22).

Example 16 Gastroliths were dissected from endocrinologically-induced premolt crayfish, weighed, rinsed with distilled water and kept at -20 C. After the external io layer of the gastrolith was scraped to eliminate any residual external material, the gastroliths were frozen using liquid nitrogen and ground to powder using a mortar and pestle. Demineralization was performed by stirring of each gram of gastrolith powder was in 20 ml of 0.02 M ammonium acetate, 0.5 M EGTA, pH 7.0, on ice. When the CaCO3 dissolution completed, the suspension was centrifuged (2000 rpm, 15-20 min, 4 C) and the supernatant was collected. The residual insoluble matrix (ISM) was used as additive to the calcifying solution (step ii). 200 l of the ISM (estimated: -gg protein) were added to 10 ml of the crystallization mixture comprising 10 mM CaC12 and 10 mM Na2CO3, followed by air flow dehydration. RS showed ACC (Fig. 23).

Example 17 The conditions as described in Example 16 were modified by changing the final concentrations of CaC12 and Na2CO3 from 10 mM to 20 mM, and the volume of ISM to 100 pl (-15 g protein), while dehydrating by means of lyophilizing. RS showed ACC (Fig. 24).

Example 18 The ISM was treated with various proteolytic enzymes in order to release the chitin binding proteins (either hydrogen or covalent bonding) from the

-25-chitinous insoluble phase, and to demonstrate the activity of resulting peptides in ACC induction and stabilization (Fig. 25).

28 ml of ammonium acetate (2 mM) were added to 7 ml of ISM. From this solution 10 ml were mixed with 10 ml of trypsin (3.8mg/ml) in ammonium acetate (2 mM). The suspensions of the ISM with the proteolytic enzymes were incubated for 2 hr at 4 C under vortexed condition. After the incubation the vials were centrifuged for 5 minutes at 4000 rpm. The supernatant which contained the ISM digested proteins was removed; 1ml of the supernatant (equivalent to 100 l of insoluble matrix and to -150 g protein was added to 10m1 of CaC12 (10mM). 100 0 of 1M Na2CO3 (final concentration: 10mM) were added following an intensive shaking. The vial was centrifuged for 5 min at 4000 RPM, the precipitation was smeared over a glass slide and instantly dried with air flow. RS showed ACC (Fig. 25). The sample was stored at room temperature and tested for ACC stability seven months after the precipitation (Fig. 30).

Example 19 28 ml of ammonium acetate (2 mM) were added to 7 ml of ISM. From this solution 10 ml were mixed with 10 ml of protease from Streptomyces griseus (Sigma P6911, 0.6mg/ml) in ammonium acetate (2 mM). The suspensions of the ISM with the proteolytic enzymes were incubated for 2 hr at 4 C under vortexing. After the incubation the vials were centrifuged for 5 minutes at 4000 rpm. The supernatant which contained the ISM digested proteins was removed; 1ml of the supernatant was added to 10ml of CaC12 (10mM). 100 l of 1M Na2CO3 (final concentration: 10mM) were added following an intensive shaking. The vial was centrifuged for 5 min at 4000 RPM, the precipitation was smeared over a glass slide and instantly dried with air flow. RS showed the ACC peak (at 1080), and additional secondary peak, possibly of calcium phosphate (peak at 950) (Fig. 26). The sample was stored at room

-26-temperature and tested for ACC stability seven months after the precipitation (Fig. 31).

Example 20 28 ml of ammonium acetate (2 mM) were added to 7 ml of ISM. From this solution 10 ml were mixed with 10 ml of papain (0.26mg/ml) in ammonium acetate (2 mM). The suspensions of the ISM with the proteolytic enzymes were incubated for 2 hr at 4 C under vortexed condition. After the incubation the vials were centrifuged for 5 minutes at 4000 rpm. The supernatant which to contain now the ISM digested proteins was removed; lml of the supernatant was added to 10ml of CaC12 (10mM). 100 pl of 1M Na2CO3 (final concentration: 10mM) were added following an intensive shaking. The vial was centrifuged for 5 min at 4000 RPM, the precipitation was smeared over a glass slide and instantly dried with air flow. RS showed ACC, and possibly calcium phosphate (Fig. 27). The sample was stored at room temperature and tested for ACC stability seven months after the precipitation (Fig. 32).

While this invention has been described in terms of some specific examples, many modifications and variations are possible. It is therefore understood that within the scope of the appended claims, the invention may be realized otherwise than as specifically described.

Claims (16)

CLAIMS:

1. A composition comprising amorphous calcium carbonate (ACC) and at least one phosphorylated amino acid.

2. The composition according to claim 1, wherein said phosphorylated amino acid is phosphorylated serine or phosphorylated threonine.

3. A method of preparing stable amorphous calcium carbonate, comprising mixing in aqueous phase in any order a soluble salt comprising calcium, a carbonate source, and a phosphorylated amino acid.

4. A pharmaceutical formulation comprising a composition according to claim 1 or 2.

5. The pharmaceutical formulation of claim 4, further comprising other components selected from the group consisting of chitin, chitosan, and fillers.

6. A nutraceutical formulation comprising the composition of claim 1 or 2.

7. A pharmaceutical formulation according to claim 4 or 5, for treating conditions selected from the group consisting of pain, proliferative diseases, neurological disorders, immunologic disorders, cardiovascular diseases, pulmonary diseases, nutritional disorders, reproductive disorders, musculoskeletal disorders, and dental problems.

8. A pharmaceutical formulation according to claim 6, wherein said proliferative disease is breast carcinoma or bronchogenic carcinoma.

9. A pharmaceutical formulation according to claim 6, wherein said pain is selected from postoperative pain, pain after injury, pain associated with cancer, and neuropathic pain.

10. A pharmaceutical formulation according to claim 6, wherein said neurologic disorder is selected from demyelinating diseases, dementias, and movement disorders.

11. A pharmaceutical formulation according to claim 6, wherein said condition is a degenerative disease selected from multiple sclerosis, Alzheimer's disease, and Parkinson's disease.

12. A pharmaceutical formulation according to claim 6, wherein said condition comprises a bone disorder or a bone marrow disorder.

13. A pharmaceutical formulation according to claim 6, wherein said disorder comprises fracture or osteoporosis.

14. A pharmaceutical formulation according to claim 6, wherein said condition is a neurodegenerative disorder.

15. Use of a composition according to claim 1 or 2, for treating a condition selected from the group consisting of pain, proliferative diseases, neurological disorders, immunologic disorders, cardiovascular diseases, pulmonary diseases, nutritional disorders, reproductive disorders, musculoskeletal disorders, and dental problems.

16. Use of a composition according to claim 1 or 2, for the manufacture of a medicament for the treatment of a condition selected from the group consisting of pain, proliferative diseases, neurological disorders, immunologic disorders, cardiovascular diseases, pulmonary diseases, nutritional disorders, reproductive disorders, musculoskeletal disorders, and dental problems.